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717337001: Syndromic hypoplasia of orbital border (disorder)


Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3309097011 Syndromic hypoplasia of orbital border (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3309098018 Syndromic orbital border hypoplasia en Synonym Active Case insensitive SNOMED CT core
3309099014 Urrets Zavalia syndrome en Synonym Active Case sensitive SNOMED CT core
3309100018 Syndromic hypoplasia of orbital border en Synonym Active Case insensitive SNOMED CT core
3309101019 Syndromic orbital border hypoplasia is a rare disorder observed in two families to date with characteristics of agenesis of the orbital margin, varying defects of the lacrimal passages, hypoplasia of the palpebral skin and tarsal plates and atresia of the nasolacrimal duct. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Syndromic orbital border hypoplasia Occurrence Congenital true Inferred relationship Some 1
Syndromic orbital border hypoplasia Pathological process Pathological developmental process true Inferred relationship Some 1
Syndromic orbital border hypoplasia Associated morphology Hypoplasia true Inferred relationship Some 1
Syndromic orbital border hypoplasia Pathological process Pathological developmental process true Inferred relationship Some 2
Syndromic orbital border hypoplasia Associated morphology Morphologically abnormal structure true Inferred relationship Some 2
Syndromic orbital border hypoplasia Finding site Orbital margin structure true Inferred relationship Some 1
Syndromic orbital border hypoplasia Is a Developmental hereditary disorder true Inferred relationship Some
Syndromic orbital border hypoplasia Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Syndromic orbital border hypoplasia Is a Congenital anomaly of orbit true Inferred relationship Some
Syndromic orbital border hypoplasia Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some
Syndromic orbital border hypoplasia Is a Orbital margin finding true Inferred relationship Some
Syndromic orbital border hypoplasia Is a Hereditary disorder of the visual system true Inferred relationship Some
Syndromic orbital border hypoplasia Occurrence Congenital true Inferred relationship Some 2
Syndromic orbital border hypoplasia Finding site Face structure true Inferred relationship Some 2
Syndromic orbital border hypoplasia Occurrence Congenital false Inferred relationship Some 3
Syndromic orbital border hypoplasia Associated morphology Hypoplasia false Inferred relationship Some 2
Syndromic orbital border hypoplasia Finding site Orbital margin structure false Inferred relationship Some 2
Syndromic orbital border hypoplasia Associated morphology Developmental abnormality false Inferred relationship Some 3
Syndromic orbital border hypoplasia Finding site Face structure false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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